Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 932 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
932 in last 12 months

Showing 46981–47000 of 50,223 recalls

Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 45cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Aspiration Needle Tip. Recalled...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

Recalled Item: GE Recalled by GE Healthcare, LLC Due to GE Healthcare has recently become...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

Recalled Item: GE PET Discovery 610 Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice¿ Rayon Tipped OB/GYN Applicator Recalled by Owens & Minor...

The Issue: Owens & Minor Distribution, Inc. is conducting a market withdrawal of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand RPM Respiratory Gating System Recalled by Varian Medical...

The Issue: Varian has identified an anomaly with the RPM Respiratory Gating System...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...

The Issue: Stryker Orthopaedics received a report that a label on the external...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2013· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...

The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
FoodMarch 25, 2013· Decoty Coffee Company, Inc

Recalled Item: Taco Seasoning Recalled by Decoty Coffee Company, Inc Due to Undeclared...

The Issue: Recently, DeCoty Taco Seasoning, 1.25 lb (Lot numbers 010111-021313) and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Testosterone Cypionate/Testosterone Enanthate Injection Recalled by Pallimed...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Methylcobalamin PF Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: DMSO Aqueous Irrigation 50% Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Atropine Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Nandrolone Decanoate Injectable Recalled by Pallimed Solutions Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Trimix Injection Recalled by Pallimed Solutions Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Alprostadil IN NS Injection Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: MIC with B6 and B12 Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund